APX-PARACETAMOL/CODEINE paracetamol 500 mg and codeine phosphate hemihydrate 30 mg tablet blister pack

국가: 오스트레일리아

언어: 영어

출처: Department of Health (Therapeutic Goods Administration)

지금 구매하세요

환자 정보 전단 환자 정보 전단 (PIL)
09-12-2021
제품 특성 요약 제품 특성 요약 (SPC)
09-12-2021
공공 평가 보고서 공공 평가 보고서 (PAR)
11-07-2020

유효 성분:

paracetamol, Quantity: 500 mg; codeine phosphate hemihydrate, Quantity: 30 mg

제공처:

Sanofi-Aventis Australia Pty Ltd

약제 형태:

Tablet, uncoated

구성:

Excipient Ingredients: potassium sorbate; maize starch; povidone; purified talc; stearic acid; magnesium stearate; microcrystalline cellulose; croscarmellose sodium; pregelatinised maize starch

관리 경로:

Oral

패키지 단위:

20 tablets, 10 tablets

처방전 유형:

(S4) Prescription Only Medicine

치료 징후:

APX-Paracetamol/Codeine is indicated for the short-term management of severe pain for which other treatment options have failed, are contraindicated, not tolerated or are otherwise inappropriate to provide sufficient management of pain.

제품 요약:

Visual Identification: White to off-white, capsule shaped tablets, marked "P" and "F" either side of a scoreline on one side and plain on the other. Dimensions: 17.46 x 7.14 x 6.05mm.; Container Type: Blister Pack; Container Material: PVC/Al; Container Life Time: 5 Years; Container Temperature: Store below 25 degrees Celsius

승인 상태:

Registered

승인 날짜:

2020-06-29

환자 정보 전단

                                APX-PARACETAMOL/CODEINE
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CONSUMER MEDICINE INFORMATION (CMI) SUMMARY
The full CMI on the next page has more details. If you are worried
about using this medicine, speak to your doctor or pharmacist.
WARNING: Important safety information is provided in a boxed warning
in the full CMI. Read before using this medicine.
1.
WHY AM I TAKING APX-PARACETAMOL/CODEINE?
APX-Paracetamol/Codeine contains the active ingredients paracetamol
and codeine phosphate hemihydrate. APX-Paracetamol/
Codeine is used to relieve severe pain. For more information, see
Section 1. Why am I using APX-Paracetamol/Codeine? in the full
CMI.
2.
WHAT SHOULD I KNOW BEFORE I TAKE APX-PARACETAMOL/CODEINE?
Do not use if you have ever had an allergic reaction to
APX-Paracetamol/Codeine or any of the ingredients listed at the end of
the CMI. TALK TO YOUR DOCTOR IF YOU HAVE ANY OTHER MEDICAL CONDITIONS,
TAKE ANY OTHER MEDICINES, OR ARE PREGNANT OR PLAN
TO BECOME PREGNANT OR ARE BREASTFEEDING. You may develop addiction,
dependence and tolerance. For more information, see
Section 2. What should I know before I use APX-Paracetamol/Codeine? in
the full CMI.
3.
WHAT IF I AM TAKING OTHER MEDICINES?
Some medicines may interfere with APX-Paracetamol/Codeine and affect
how it works. A list of these medicines is in Section 3.
What if I am taking other medicines? in the full CMI.
4.
HOW DO I TAKE APX-PARACETAMOL/CODEINE?
The standard dose for adults is 1 or 2 tablets for severe pain, taken
every 4 to 6 hours if necessary. More instructions can be found
in Section 4. How do I use APX-Paracetamol/Codeine? in the full CMI.
5.
WHAT SHOULD I KNOW WHILE TAKING APX-PARACETAMOL/CODEINE?
THINGS YOU
SHOULD DO
•
Remind any doctor, dentist or pharmacist you visit that you are using
APX-Paracetamol/Codeine.
•
Talk to your doctor about pain control if the medicine is not helping.
•
Tell your doctor if you become pregnant while taking
APX-Paracetamol/Codeine.
THINGS YOU
SHOULD NOT DO
•
Do not take more than the recommende
                                
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제품 특성 요약

                                apx-para-cod-ccdsv5-piv3-03dec21
1
AUSTRALIAN PRODUCT INFORMATION – APX-
PARACETAMOL/CODEINE (PARACETAMOL, CODEINE
PHOSPHATE HEMIHYDRATE)
1
NAME OF THE MEDICINE
Paracetamol and codeine phosphate hemihydrate
WARNINGS
LIMITATIONS OF USE
BECAUSE OF THE RISKS ASSOCIATED WITH THE USE OF OPIOIDS, APX-
PARACETAMOL/CODEINE SHOULD ONLY BE USED IN PATIENTS FOR WHOM OTHER
TREATMENT
OPTIONS, INCLUDING NON-OPIOID ANALGESICS, ARE INEFFECTIVE, NOT
TOLERATED OR
OTHERWISE INADEQUATE TO PROVIDE APPROPRIATE MANAGEMENT OF PAIN (SEE
SECTION
4.4 SPECIAL WARNINGS AND PRECAUTIONS FOR USE).
HAZARDOUS AND HARMFUL USE
APX-PARACETAMOL/CODEINE POSES RISKS OF HAZARDOUS AND HARMFUL USE WHICH
CAN
LEAD TO OVERDOSE AND DEATH. ASSESS THE PATIENT’S RISK OF HAZARDOUS
AND HARMFUL
USE BEFORE PRESCRIBING AND MONITOR THE PATIENT REGULARLY DURING
TREATMENT (SEE
SECTION 4.4. SPECIAL WARNINGS AND PRECAUTIONS FOR USE).
LIFE THREATENING RESPIRATORY DEPRESSION
SERIOUS, LIFE-THREATENING OR FATAL RESPIRATORY DEPRESSION MAY OCCUR
WITH THE USE
OF APX-PARACETAMOL/CODEINE. BE AWARE OF SITUATIONS WHICH INCREASE THE
RISK OF
RESPIRATORY DEPRESSION, MODIFY DOSING IN PATIENTS AT RISK AND MONITOR
PATIENTS
CLOSELY, ESPECIALLY ON INITIATION OR FOLLOWING A DOSE INCREASE (SEE
SECTION 4.4
SPECIAL WARNINGS AND PRECAUTIONS FOR USE).
CONCOMITANT USE OF BENZODIAZEPINES AND OTHER CENTRAL NERVOUS SYSTEM
(CNS)
DEPRESSANTS, INCLUDING ALCOHOL
CONCOMITANT USE OF OPIOIDS WITH BENZODIAZEPINES, GABAPENTINOIDS,
ANTIHISTAMINES, TRICYCLIC ANTIDEPRESSANTS, ANTIPSYCHOTICS, CANNABIS OR
OTHER
CENTRAL NERVOUS SYSTEM (CNS) DEPRESSANTS, INCLUDING ALCOHOL, MAY
RESULT IN
PROFOUND SEDATION, RESPIRATORY DEPRESSION, COMA, AND DEATH. LIMIT
DOSAGES AND
DURATIONS TO THE MINIMUM REQUIRED; AND MONITOR PATIENTS FOR SIGNS AND
SYMPTOMS OF RESPIRATORY DEPRESSION AND SEDATION. CAUTION PATIENTS NOT
TO DRINK
ALCOHOL WHILE TAKING APX-PARACETAMOL/CODEINE.
apx-para-cod-ccdsv5-piv3-03dec21
2
2
QUALITATIVE AND QUANTITATIVE COMPOSITION
Each capsule-shaped tablet contains paracetamol 500 mg, codeine
phosphate hemihydr
                                
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